drjobs Lead Manufacturing Technician

Lead Manufacturing Technician

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1 Vacancy
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Job Location drjobs

Saint Louis - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Work Schedule

Rotational shift nights/weekends

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.)

Job Description

Discover Impactful Work:

Thermo Fisher Scientific seeks a Lead Manufacturing Technician to help produce Commercial and Clinical Biologics in a GMP facility.

A day in the Life:

  • Own the execution of routine and nonroutine cleaning of operational areas per work instructions and/or SOPs with a focus on right the first time executions.
  • Maintain supplies equipment logbooks and data in accordance with site SOPs and policies.
  • Lead the assembly and cleaning activities of manufacturingrelated equipment per work instructions and/or SOPs.
  • Document all activities to meet cGMP requirements. Perform daily logbook reviews tasks and database updates.
  • Complete preventative maintenance and work notifications tasks on time. Conduct equipment testing and routine troubleshooting.
  • Coordinate and perform timely consumption of materials and completion of quality documentation in appropriate systems.
  • Identify deviations aid in investigations/root cause analysis and provide input on major/critical deviations.
  • Complete validation protocols with minimal supervision or direction.
  • Schedule activities and coordinate the shift huddle in the absence of the supervisor. Act as a liaison with other groups within the manufacturing organization and as a Subject Matter Expert on various techniques.
  • Participate in shift exchanges oneonone meetings and attend necessary meetings to facilitate area needs based on changes.
  • Practice and promote safe work habits and adhere to safety procedures and guidelines.
  • Provide feedback on document revisions and/or document management including batch production records and manufacturing procedures.
  • Seek and welcome feedback and respond to mentoring.

Keys to Success:

Education:

  • HS Diploma or equivalent experience required; bachelors degree or equivalent experience preferred

Experience:

0 4 years relevant work experience required based on education

  • Experience in a cGMP environment preferred

Knowledge Skills Abilities:

  • Knowledge of cGMP practices aseptic techniques or chemical concepts preferred

Required Experience:

IC

Employment Type

Full-Time

Company Industry

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